NM_024675.4(PALB2):c.876A>G (p.Gln292=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 2, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001179427.2
Allele description [Variation Report for NM_024675.4(PALB2):c.876A>G (p.Gln292=)]
NM_024675.4(PALB2):c.876A>G (p.Gln292=)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
nucleoside triphosphate pyrophosphatase [Musicola paradisiaca]
nucleoside triphosphate pyrophosphatase [Musicola paradisiaca]gi|506335609|ref|WP_015855328.1|Protein
-
regulator of nonsense transcripts 3A isoform X2 [Homo sapiens]
regulator of nonsense transcripts 3A isoform X2 [Homo sapiens]gi|767979384|ref|XP_011533147.1|Protein
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023